Evidence map›Paper›PMID 31276542›Full record

ArticlePloS one2019

Optimizing the alignment of thermoresponsive poly(N-isopropyl acrylamide) electrospun nanofibers for tissue engineering applications: A factorial design of experiments approach.

Rachel E Young, Jodi Graf, Isabella Miserocchi, Ryan M Van Horn, Melissa B Gordon, Christopher R Anderson, Lauren S Sefcik

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.5field-weighted citation impact, top 20% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Review
  8. Article
  9. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 1 institution in 1 country.

Rachel E YoungDepartment of Chemical and Biomolecular Engineering, Lafayette College, Easton, Pennsylvania, United States of America.
Jodi GrafDepartment of Chemical and Biomolecular Engineering, Lafayette College, Easton, Pennsylvania, United States of America.
Isabella MiserocchiDepartment of Chemical and Biomolecular Engineering, Lafayette College, Easton, Pennsylvania, United States of America.
Ryan M Van HornDepartment of Chemical and Biomolecular Engineering, Lafayette College, Easton, Pennsylvania, United States of America.ORCID 0000-0002-1065-7378
Melissa B GordonDepartment of Chemical and Biomolecular Engineering, Lafayette College, Easton, Pennsylvania, United States of America.ORCID 0000-0001-5881-3432
Christopher R AndersonDepartment of Chemical and Biomolecular Engineering, Lafayette College, Easton, Pennsylvania, United States of America.
Lauren S SefcikDepartment of Chemical and Biomolecular Engineering, Lafayette College, Easton, Pennsylvania, United States of America.ORCID 0000-0003-1130-2605
Lafayette College · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Thermoresponsive polymers, such as poly(N-isopropyl acrylamide) (PNIPAM), have been identified and used as cell culture substrates, taking advantage of the polymer's lower critical solution temperature (LCST) to mechanically harvest cells. This technology bypasses the use of biochemical enzymes that cleave important cell-cell and cell-matrix interactions. In this study, the process of electrospinning is used to fabricate and characterize aligned PNIPAM nanofiber scaffolds that are biocompatible and thermoresponsive. Nanofiber scaffolds produced by electrospinning possess a 3D architecture that mimics native extracellular matrix, providing physical and chemical cues to drive cell function and phenotype. We present a factorial design of experiments (DOE) approach to systematically determine the effects of different electrospinning process parameters on PNIPAM nanofiber diameter and alignment. Results show that high molecular weight PNIPAM can be successfully electrospun into both random and uniaxially aligned nanofiber mats with similar fiber diameters by simply altering the speed of the rotating mandrel collector from 10,000 to 33,000 RPM. PNIPAM nanofibers were crosslinked with OpePOSS, which was verified using FTIR. The mechanical properties of the scaffolds were characterized using dynamic mechanical analysis, revealing an order of magnitude difference in storage modulus (MPa) between cured and uncured samples. In summary, cross-linked PNIPAM nanofiber scaffolds were determined to be stable in aqueous culture, biocompatible, and thermoresponsive, enabling their use in diverse cell culture applications.

Indexed as

AcrylamidesAcrylic ResinsBiocompatible MaterialsExtracellular MatrixNanofibersPolymersTissue EngineeringTissue ScaffoldsAcrylamidesAcrylic ResinsBiocompatible MaterialsPolymerspoly-N-isopropylacrylamide

Identifiers

PMID31276542
PMCPMC6611625
OpenAlexW2953951822

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.